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Crystal structure of crotonase from clostridium acetobutylicum

Analyse Crystal structure of crotonase from clostridium acetobutylicum in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5Z7R
Type
protein
Length
762 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Short-chain-enoyl-CoA hydratase
EC
4.2.1.150
UniProt
P52046
Pockets
8 · best druggability 0.85

Structure

x-ray diffraction · 1 distinct chain · 55% helix, 17% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, CShort-chain-enoyl-CoA hydratase (EC 4.2.1.150)protein25455% helix, 17% strandP52046

Pockets

8 pockets found on a 1 Å grid, 4 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
18120.850.8884empty
22360.590.8036empty
31730.570.8132empty
41570.570.8128empty
51030.430.7716empty

Interfaces

3 interfaces between chains.

  • B–C · 2154 Ų buried · 32 hydrogen bonds · protein-protein
  • A–C · 2119 Ų buried · 32 hydrogen bonds · protein-protein
  • A–B · 2108 Ų buried · 27 hydrogen bonds · protein-protein

Compared structures

  • 5Z7R · Crystal structure of crotonase from Clostridium acetobutylicum · the same entry in another collection · chain A against A, TM-score 1.00
  • P52046 · AlphaFold monomer V2.0 prediction for short-chain-enoyl-CoA hydratase (P52046) · a predicted model of the same protein · chain A against A, TM-score 0.98

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